医学
CD20
肿瘤揭穿
内科学
弥漫性大B细胞淋巴瘤
胃肠病学
嵌合抗原受体
淋巴瘤
临床研究阶段
化疗
肿瘤科
耐火材料(行星科学)
免疫疗法
癌症
生物
天体生物学
作者
Yao Wang,Wen‐Ying Zhang,Qingwang Han,Yang Liu,Hanren Dai,Yelei Guo,Jian Bo,Hui Fan,Yan Zhang,Weidong Han,Meixia Chen,Kaichao Feng,Quanshun Wang,Xiaobing Fu,Weidong Han
标识
DOI:10.1016/j.clim.2014.10.002
摘要
We conducted a trial testing a CD20-specific CAR coupled with CD137 and the CD3ζ moiety in patients with chemotherapy refractory advanced diffuse large B cell lymphomas (DLBCL). Seven patients were enrolled. One of the two patients with no bulky tumor obtained a 14-month durable and ongoing complete remission by cell infusion only, and another attained a 6-month tumor regression. Four of five patients with bulky tumor burden were evaluable for clinical efficacy, three of which attained 3- to 6-month tumor regression. Delayed toxicities related to cell infusion are directly correlated to tumor burden and tumor-harboring sites, and mainly included cytokine release symptoms, tumor lysis symptoms, massive hemorrhage of the alimentary tract and aggressive intrapulmonary inflammation surrounding extranodal lesions. These results show firstly that anti-CD20 CART cells can cause prolonged tumor regression in combination with debulking conditioning regimens for advanced DLBCL. This study is registered at www.clinicaltrials.gov as NCT01735604.
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